CHEBI:66219 - thiazomycin

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ChEBI Name thiazomycin
ChEBI ID CHEBI:66219
Definition A heterodetic cyclic peptide isolated from Amycolatopsis fastidiosa.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C61H58N14O18S5
Net Charge 0
Average Mass 1435.52100
Monoisotopic Mass 1434.26571
InChI InChI=1S/C61H58N14O18S5/c1-22(48(62)78)63-49(79)31-18-97-57(68-31)42-36(77)11-27-41(70-42)30-16-95-55(65-30)29-15-90-59(84)44-28-14-88-45(46(60(85)89-13-26-9-8-10-35(38(26)28)75(44)86)93-37-12-61(5)47(25(4)92-37)74(6)21-91-61)43(58-69-32(19-98-58)50(80)64-29)73-52(82)34-20-96-56(67-34)40(24(3)87-7)72-53(83)39(23(2)76)71-51(81)33-17-94-54(27)66-33/h8-11,16-20,23,25,29,37,39,43,45-47,76-77,86H,1,12-15,21H2,2-7H3,(H2,62,78)(H,63,79)(H,64,80)(H,71,81)(H,72,83)(H,73,82)/b40-24+/t23-,25+,29+,37+,39+,43+,45+,46+,47-,61+/m1/s1
InChIKey GYOHFSLEKIIJMU-UMNFMQIXSA-N
SMILES CO\C(C)=C1\NC(=O)[C@@H](NC(=O)c2csc(n2)-c2cc(O)c(nc2-c2csc(n2)[C@@H]2COC(=O)c3c4CO[C@@H]([C@H](NC(=O)c5csc1n5)c1nc(cs1)C(=O)N2)[C@H](O[C@H]1C[C@]2(C)OCN(C)[C@@H]2[C@H](C)O1)C(=O)OCc1cccc(n3O)c41)-c1nc(cs1)C(=O)NC(=C)C(N)=O)[C@@H](C)O
Metabolite of Species Details
Amycolatopsis fastidiosa (NCBI:txid1816) See: PubMed
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Biological Role(s): antimicrobial agent
A substance that kills or slows the growth of microorganisms, including bacteria, viruses, fungi and protozoans.
bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
antibacterial agent
A substance (or active part thereof) that kills or slows the growth of bacteria.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing thiazomycin (CHEBI:66219) has role antibacterial agent (CHEBI:33282)
thiazomycin (CHEBI:66219) has role antimicrobial agent (CHEBI:33281)
thiazomycin (CHEBI:66219) has role bacterial metabolite (CHEBI:76969)
thiazomycin (CHEBI:66219) is a heterodetic cyclic peptide (CHEBI:24533)
Registry Number Type Source
12681378 Reaxys Registry Number Reaxys
Citation Waiting for Citations Type Source
17917239 PubMed citation Europe PMC
Last Modified
28 October 2014